Determination of function in the isolated working mouse heart: Issues in experimental design

被引:23
作者
Gauthier, NS
Matherne, GP
Morrison, RR
Headrick, TP
机构
[1] Univ Virginia, Hlth Sci Ctr, Dept Pediat, Charlottesville, VA 22908 USA
[2] Univ Virginia, Hlth Sci Ctr, Cardiovasc Res Ctr, Charlottesville, VA 22908 USA
[3] Griffith Univ, Rotary Ctr Cardiovasc Res, Nathan, Qld 4111, Australia
关键词
afterload; mouse heart; preload; working heart;
D O I
10.1006/jmcc.1997.0610
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The goal of the present study was to compare two common types of isolated working mouse heart models, setting afterload either with (1) a hydrostatic fluid column, or (2) a mechanical resistor. Cardiovascular function in both models was determined by volume-and pressure-loading protocols. During volume loading, both models demonstrated a fixed degree of outflow resistance from the 20-gauge rigid aortic cannula resulting in a small predictable rise in left-ventricular pressure. In the mechanical resistor model, volume loading resulted in a marked increase in afterload, with a >50% increase from baseline aortic pressure. This altered ventricular mechanics, resulting in twice the expected change in dP/dt during volume loading. Additionally, coronary flow in the mechanical resistor model rose by more than four-fold in parallel to the increased preload. When using the fluid column model, however. aortic pressure was unchanged and coronary now remained stable. During pressure loading, no significant differences in ventricular mechanics or coronary flow between the mechanical resistor and fluid column models were noted. When mouse hemodynamic data were compared to that from larger species, mouse hearts had similar cardiac function and efficiency with higher MVO2 and coronary flows. in summary, the hydrostatic fluid column isolated working mouse heart model is preferred over the mechanical resistor model for studying murine cardiac function. Further, use of this model provides hemodynamic data that is consistent with larger species, albeit with higher MVO2 and basal coronary now, and should allow relevant study of mouse cardiac physiology. (C) 1998 Academic Press Limited.
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页码:453 / 461
页数:9
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